Skip to content
left end
left end
right end

The National Haemoglobinopathy Registry (NHR)

The National Haemoglobinopathy Registry is a database of patients with red cell disorders living in the UK. This new database collects data, which is required by the Department of Health from Haemoglobinopathy centres. The central aim of the registry is to improve patient care.

Letters with more detail about NHR were sent out to all existing patients. New patients will receive a letter once they are registered with us and have not previously been registered by a different centre in England.